首页> 美国卫生研究院文献>American Journal of Physiology - Cell Physiology >High potassium promotes mutual interaction between (pro)renin receptor and the local renin-angiotensin-aldosterone system in rat inner medullary collecting duct cells
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High potassium promotes mutual interaction between (pro)renin receptor and the local renin-angiotensin-aldosterone system in rat inner medullary collecting duct cells

机译:高钾促进大鼠内髓收集管细胞中(原)肾素受体与局部肾素-血管紧张素-醛固酮系统之间的相互作用

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摘要

(Pro)renin receptor (PRR) is predominantly expressed in the collecting duct (CD) with unclear functional implication. It is not known whether CD PRR is regulated by high potassium (HK). Here, we aimed to investigate the effect of HK on PRR expression and its role in regulation of aldosterone synthesis and release in the CD. In primary rat inner medullary CD cells, HK augmented PRR expression and soluble PPR (sPRR) release in a time- and dose-dependent manner, which was attenuated by PRR small interfering RNA (siRNA), eplerenone, and losartan. HK upregulated aldosterone release in parallel with an increase of CYP11B2 (cytochrome P-450, family 11, subfamily B, polypeptide 2) protein expression and upregulation of medium renin activity, both of which were attenuated by a PRR antagonist PRO20, PRR siRNA, eplerenone, and losartan. Similarly, prorenin upregulated aldosterone release and CYP11B2 expression, both of which were attenuated by PRR siRNA. Interestingly, a recombinant sPRR (sPRR-His) also stimulated aldosterone release and CYP11B2 expression. Taken together, we conclude that HK enhances a local renin-angiotensin-aldosterone system (RAAS), leading to increased PRR expression, which in turn amplifies the response of the RAAS, ultimately contributing to heightened aldosterone release.
机译:(Pro)肾素受体(PRR)主要在集管(CD)中表达,功能含义不清楚。尚不清楚CD PRR是否受高钾(HK)调节。在这里,我们旨在调查HK对PRR表达的影响及其在CD中醛固酮合成和释放调节中的作用。在原代大鼠髓质CD细胞中,HK以时间和剂量依赖性方式增加PRR表达和可溶性PPR(sPRR)释放,这被PRR小干扰RNA(siRNA),依普利农和氯沙坦减弱。 HK与CYP11B2(细胞色素P-450,家族11,亚家族B,多肽2)蛋白质表达的增加和醛固酮中等表达的上调并行,同时被PRR拮抗剂PRO20,PRR siRNA,依普利酮减弱。和losartan。同样,肾上腺素原上调了醛固酮的释放和CYP11B2的表达,两者均被PRR siRNA减弱。有趣的是,重组sPRR(sPRR-His)也刺激了醛固酮的释放和CYP11B2的表达。两者合计,我们得出结论,HK增强了局部肾素-血管紧张素-醛固酮系统(RAAS),导致PRR表达增加,继而放大了RAAS的反应,最终导致醛固酮释放增加。

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